CAS: 69806-50-4; Fluazifop-Butyl

该化合物是一种选择性的系统性除草剂,主要用于控制各种作物中的年度和常年草草,属于除草剂的丙氧酚类和功能,抑制对植物中脂肪酸合成至关重要的酶丙基-可口氨基碳斗酶,抑制了易感染的草种的生长,同时使宽叶片植物基本上不受影响.氟氮素丁基通常在出现后应用,使其能针对积极生长的草.该化合物的特点是它对哺乳动物和鸟类的毒性较低,使其在农业环境中成为首选的首选.该化合物一般是作为乳油或液体配方来配制,以便于施用.环境持久性是中度的,并且会因土壤中的微生物活动而退化.适当处理和应用对于最大限度地减少潜在的环境影响和确保有效控制杂草至关重要.与所有除草剂一样,遵守安全准则和规章对于负责任的使用至关重要.

结构式图片

欧盟法规

统一分类与标签ECHA物质食品接触材料-禁用CMR物质ECHA物质化妆品禁用物质清单C&L通报欧盟农药活性物质工作场所安全标识要求REACH预注册废弃物危险特性清单

上下游产品

CAS号80776-65-4 n-butyl 2-[4-(5... | CAS号81947-94-6 n-butyl 2-(4-hy... | CAS号52334-81-3 2-氯-5-三氟甲基吡啶

合成工艺路线路线简述

  • 合成目标产物 Fluazifop-Butyl 主要起始原料 Propanoic Acid, 2-(4-Hydroxyphenoxy)-, Butyl Ester And 2-Chloro-5-Trifluoromethylpyridine
  • (文献来源)合成步骤主要原料 Propanoic Acid, 2-(4-Hydroxyphenoxy)-, Butyl Ester 和 2-Chloro-5-Trifluoromethylpyridine
📜N-Butyl 2-[4-(5-Trifluoromethylpyrid-2-Yloxy)Phenoxy]Acrylate置于钯体系中,用 正丁醇 作为反应溶剂,化学反应生成 吡氟禾草灵
参考文献:A Process For Preparing 2-Pyridinyloxyphenoxy-Lower-Alkanoates
标题:A Process For Preparing 2-Pyridinyloxyphenoxy-Lower-Alkanoates
摘要:这项发明涉及一种制备吡啶氧基苯氧基丙烷羧酸及其衍生物的过程,以及在该过程中有用的中间体.

海关参考信息

专利信息


专利号:US-4658031-A
优先权日:1982-10-07
标 题:Synthesis of 2-substituted-5-methyl-pyridines and intermediates therefor
发明人:HARTMANN LUDWIG A; STEPHEN JOHN F
权利人:ICI AMERICA INC
摘要:A process for the synthesis of compounds which are known intermediates for the pyridyloxyphenoxy herbicies as well as intermediates used in the process. Propionaldehyde and an acrylic compound, two readily available starting materials, are reacted to form a 2-formylpentanoic compound which is cyclized to a dihydro pyridone which is then oxidized to the 2-hydroxy pyridine. The hydroxypyridine may be halogenated to a 2-halopyridine.

专利号:US-4584380-A
优先权日:1982-10-07
标 题:Synthesis of 2-substituted-5-methyl-pyridines and intermediates therefor
发明人:HARTMANN LUDWIG A; STEPHEN JOHN F
权利人:ICI AMERICA INC
摘要:A process for the synthesis of compounds which are known intermediates for the pyridyloxyphenoxy herbicides as well as intermediates used in the process. Propionaldehyde and an acrylic compound, two readily available starting materials, are reacted to form a 2-formylpentanoic compound which is cyclized to a dihydro pyridone which is then oxidized to the 2-hydroxy pyridine. The hydroxypyridine may be halogenated to a 2-halopyridine.

专利号:US-4473696-A
优先权日:1982-10-07
标题:Synthesis of 2-substituted-5-methyl-pyridines
发明人:HARTMANN LUDWIG A; STEPHEN JOHN F
权利人:ICI AMERICA INC
摘要:A process for the synthesis of compounds which are known intermediates for the pyridyloxyphenoxy herbicides as well as intermediates used in the process. Propionaldehyde and an acrylic compound, two readily available starting materials, are reacted to form a 2-formylpentanoic compound which is cyclized to a dihydro pyridone which is then oxidized to the 2-hydroxy pyridine. The hydroxypyridine may be halogenated to a 2-halopyridine.

专利号:US-4687854-A
优先权日:1982-10-07
标 题 :Bispiperidone precursor of 2-substituted-5-methyl-pyridines
发明人:HARTMANN LUDWIG A; STEPHEN JOHN F
权利人:ICI AMERICA INC
摘要:A process for the synthesis of compounds which are known intermediates for the pyridyloxyphenoxy herbicides as well as intermediates used in the process. Propionaldehyde and an acrylic compound, two radily available starting materials, are reacted to form a 2-formylpentanoic compound which is cyclized to a dihydro pyridone which is then oxidized to the 2-hydroxy pyridine. The hydroxypyridine may be halogenated to a 2-halopyridine.

专利号:US-4612377-A
优先权日:1983-03-30
标题:Preparation of 2-chloro-5-methylpyridine
发明人:OSBORNE ROBERT; BAILEY KEVIN D
权利人:ICI PLC
摘要:A 2-oxo-5-methyl-5,6-dihalopiperidine is contacted in a high boiling solvent, preferably trichlorobenzene, with a stoichiometric excess, up to 70 mole % excess, of a chlorinating agent, preferably phosphorus oxychloride or phosgene, at an elevated temperature between 80 DEG and 130 DEG C. The solution of 2-chloro-5-methylpyridine so obtained may be used directly for further chlorination to form 2-chloro-5-trichloromethylpyridine with, for example, chlorine gas in the presence of a free radical initiator. This chemical intermediate is useful in the synthesis of certain herbicidal compounds.

专利号:US-5053516-A
优先权日:1984-05-23
标题 :Synthesis of 2-substituted-5-methylpyridines from methylcyclobutanecarbonitrile, valeronitrile and pentenonitrile intermediates
发明人:HARTMANN LUDWIG A; STEPHEN JOHN F
权利人:ICI AMERICA INC
摘要:3-Methyl-2-alkylamino-1-halo-1-cyano cyclobutanes are cleaved under acid conditions to form 2-halo-4-formylvaleronitrile and 4-formyl-2-pentenonitrile which can be cyclized to form 2-substituted-5-methylpyridine derivatives. These pyridine derivatives are useful as starting materials in the manufacture of herbicides such as fluazifop-butyl.

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品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


摘要:Augustijin-Beckers PWM et al; Rev Environ Contam Toxicol 137: 1-82 (1994)
摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)
摘要:40 CFR 180.411(c) (1996)
摘要:Farm Chemicals Handbook 1997. Willoughby, OH: Meister Publishing Co., 1997., p. C-170
摘要:Tomlin, C.D.S. (ed.). The Pesticide Manual - World Compendium. 10th ed. Surrey, UK: The British Crop Protection Council, 1994., p. 472
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